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Mobile Medical Apps (Is It a FDA Regulated Device?) and Cybersecurity  

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Online Compliance Panel

Mobile Medical Apps (Is It a FDA Regulated Device?) and Cybersecurity seminar agenda print utility

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This webinar will benefit professionals from the medical device sector who are responsible for Medical device software design and development and Medical device software Verification and Validation

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Seminar Summary:

With mobile platforms more user friendly, and with computers, tablets and smart phones becoming more powerful, we see an increase in the offering of apps. Some of these apps are specifically targeted to assist individuals in the management of their health and wellness, while other apps are targeted to healthcare providers as tools to assist in the delivery of care. (see full course description)

 

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Training Course Syllabus:


Objectives of the Presentation
When does your mobile app become a medical device?
When does FDA consider your mobile app a consumer product which it will not regulate?
How does FDA determine not to regulate one app versus another?
How does the new guidance impact industry?
What is FDAs position on the cybersecurity and mobile medical applications?
Why should you Attend
The FDA has released a guidance explaining how they intend to apply their regulatory authority to software applications intended for use on mobile platforms. They have defined what types of apps they consider a medical device. Apps that are medical devices must meet all FDA device requirements, however, FDA will not enforce their requirements on Mobile apps that meet the FDAs definition of a medical device but pose a low health risk.

This webinar will explain how to determine if your app is a medical device and if it will be subject to FDA requirements. The FDA approval process for a new app will be explained including FDA software validation requirements which are more extensive than just testing performance. Cybersecurity is very important for mobile apps. The FDA requirements for cybersecurity in the app design will be explained.

Areas Covered
What mobile apps are medical devices
What mobile apps will be regulated by FDA
FDA Guidance: "Mobile Medical Applications"
Review of quality system requirements from the FDA (QSRs) and the EU (ISO 13485)
Review of software development standards: ISO 62304 and FDA guidance documents
How to get a mobile app approved by FDA
Cybersecurity for mobile apps explained

Who will Benefit

This webinar will benefit professionals from the medical device sector who are responsible for Medical device software design and development Medical device software Verification and Validation Medical device project management Software Quality Assurance Regulatory Affairs Product Managers Marketing R&D and engineering staff Information Security Officers Risk Managers Compliance Officers Privacy Officers Health Information Managers Information Technology Managers Medical Office Managers Systems Managers

Seminar Summary:

With mobile platforms more user friendly, and with computers, tablets and smart phones becoming more powerful, we see an increase in the offering of apps. Some of these apps are specifically targeted to assist individuals in the management of their health and wellness, while other apps are targeted to healthcare providers as tools to assist in the delivery of care. (see full course description)

 

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